Screening and machine learning-based prediction of translation-enhancing peptides that reduce ribosomal stalling in <i>Escherichia coli</i>

We previously reported that the nascent SKIK peptide enhances translation and alleviates ribosomal stalling caused by arrest peptides (APs) such as SecM and polyproline when positioned immediately upstream of the APs in both <i>Escherichia coli in vivo</i> and <i>in vitro</i> translation systems. In this study, we conducted a comprehensive screening of translation-enhancing peptides (TEPs) using a randomized artificial tetrapeptide library. The screening focused on the ability of the peptides to suppress SecM AP-induced translational stalling in <i>E. coli</i> cells. We identified TEPs exhibiting a range of translation-enhancing activities. <i>In vitro</i> translation analysis suggested that the fourth amino acid in the tetrapeptide influences the reduction of SecM AP-mediated stalling. Additionally, we developed a machine learning model using a random forest algorithm to predict TEP activity, which showed a strong correlation with experimentally measured activities. These findings provide a compact peptide toolkit and a data-driven approach for alleviating AP-induced ribosome stalling, with potential applications in synthetic biology.

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Publication Details

Journal
RSC Chemical Biology
Published
2025-10-22
DOI
https://doi.org/10.1039/d5cb00199d
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Screening and machine learning-based prediction of translation-enhancing peptides that reduce ribosomal stalling in Escherichia coli

Chie Motono, Gentaro Yokoyama, Teruyo Ojima‐Kato, Hideo Nakano
RSC Chemical Biology
RNA and protein synthesis mechanisms
article

Screening and machine learning-based prediction of translation-enhancing peptides that reduce ribosomal stalling in Escherichia coli

Chie Motono, Gentaro Yokoyama, Teruyo Ojima‐Kato, Hideo Nakano
article en

Abstract

We previously reported that the nascent SKIK peptide enhances translation and alleviates ribosomal stalling caused by arrest peptides (APs) such as SecM and polyproline when positioned immediately upstream of the APs in both <i>Escherichia coli in vivo</i> and <i>in vitro</i> translation systems. In this study, we conducted a comprehensive screening of translation-enhancing peptides (TEPs) using a randomized artificial tetrapeptide library. The screening focused on the ability of the peptides to suppress SecM AP-induced translational stalling in <i>E. coli</i> cells. We identified TEPs exhibiting a range of translation-enhancing activities. <i>In vitro</i> translation analysis suggested that the fourth amino acid in the tetrapeptide influences the reduction of SecM AP-mediated stalling. Additionally, we developed a machine learning model using a random forest algorithm to predict TEP activity, which showed a strong correlation with experimentally measured activities. These findings provide a compact peptide toolkit and a data-driven approach for alleviating AP-induced ribosome stalling, with potential applications in synthetic biology.

RSC Chemical BiologyVol. 7(1)
Waseda University (JP), Nagoya University (JP), National Institute of Advanced Industrial Science and Technology (JP)
National Institute of Advanced Industrial Science and Technology, Japan Society for the Promotion of Science, Japan Science and Technology Agency
Openalex Percentile: Top 73%
RNA and protein synthesis mechanisms
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